NCT02073539

Brief Summary

Chest compression (CC) feedback devices are used to perform CC measurements effectively and accurately on patients in hospital beds. However, these devices do not take account of the compression of the mattress, which results in overestimation of CC depth. This study is the validation study to demonstrate that a new method using one accelerometer(U-cpr) is useful to overcome this limitation and thus measure compression depth more accurately when performing cardiopulmonary resuscitation (CPR) on patients.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
19

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2014

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 24, 2014

Completed
3 days until next milestone

First Posted

Study publicly available on registry

February 27, 2014

Completed
2 days until next milestone

Study Start

First participant enrolled

March 1, 2014

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2014

Completed
Last Updated

March 21, 2014

Status Verified

March 1, 2014

Enrollment Period

Same day

First QC Date

February 24, 2014

Last Update Submit

March 20, 2014

Conditions

Keywords

Chest compressionOne accelerometerManikin Study

Outcome Measures

Primary Outcomes (1)

  • Chest compression depth

    Primary out come is measured by Resusci Anne Modular System Skill Reporter manikin (9.89 kg, Laerdal Medical, Orpington, UK)

    Within 1day

Secondary Outcomes (1)

  • Chest compression rate

    Within 1day

Study Arms (3)

chest compression with 5cm feedback

EXPERIMENTAL

We will feedback by one accelerometer (U-cpr). U-cpr is android based smartphone application.

Device: Stryker ST104-747Device: Shinchang SB-34p

chest compression with 6cm feedback

EXPERIMENTAL

We will feedback by one accelerometer(U-cpr). U-cpr is android based smartphone application.

Device: Stryker ST104-747Device: Shinchang SB-34p

chest compression with 7cm feedback

EXPERIMENTAL

We will feedback by one accelerometer(U-cpr). U-cpr is android based smartphone application.

Device: Stryker ST104-747Device: Shinchang SB-34p

Interventions

760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US

Also known as: Transport stretcher®
chest compression with 5cm feedbackchest compression with 6cm feedbackchest compression with 7cm feedback

, 850 x 2080 mm,Shinchang Co.,Busan,ROK

Also known as: Transport stretcher®
chest compression with 5cm feedbackchest compression with 6cm feedbackchest compression with 7cm feedback

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Postgraduates year 1,2,3,4 and Emergency physicians in emergency department

You may not qualify if:

  • Wrist or Low back disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hanyang University Seoul Hospital

Seoul, 133792, South Korea

Location

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Sang hyun Lee, M.D

    Hanyang University Seoul Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical fellow

Study Record Dates

First Submitted

February 24, 2014

First Posted

February 27, 2014

Study Start

March 1, 2014

Primary Completion

March 1, 2014

Study Completion

March 1, 2014

Last Updated

March 21, 2014

Record last verified: 2014-03

Locations